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Neuroimaging features of depression-frailty phenotype in older adults: a pilot study.
Shuster, Ethan; Miles, Amy E; Heyland, Lindsay K; Calarco, Navona; Jeyachandra, Jerrold; Mansour, Salim; Voineskos, Aristotle N; Steffens, David C; Nikolova, Yuliya S; Diniz, Breno S.
Afiliação
  • Shuster E; UConn Center on Aging, University of Connecticut School of Medicine, Farmington, CT, USA.
  • Miles AE; Centre for Addiction and Mental Health, Toronto, ON, Canada.
  • Heyland LK; Centre for Addiction and Mental Health, Toronto, ON, Canada.
  • Calarco N; Centre for Addiction and Mental Health, Toronto, ON, Canada.
  • Jeyachandra J; Centre for Addiction and Mental Health, Toronto, ON, Canada.
  • Mansour S; Centre for Addiction and Mental Health, Toronto, ON, Canada.
  • Voineskos AN; Centre for Addiction and Mental Health, Toronto, ON, Canada.
  • Steffens DC; Department of Psychiatry, University of Toronto, Toronto, ON, Canada.
  • Nikolova YS; Department of Psychiatry, University of Connecticut School of Medicine, Farmington, CT, USA.
  • Diniz BS; Centre for Addiction and Mental Health, Toronto, ON, Canada.
Int Psychogeriatr ; 35(12): 717-723, 2023 Dec.
Article em En | MEDLINE | ID: mdl-36803400
OBJECTIVE: Frailty and late-life depression (LLD) often coexist and share several structural brain changes. We aimed to study the joint effect LLD and frailty have on brain structure. DESIGN: Cross-sectional study. SETTING: Academic Health Center. PARTICIPANTS: Thirty-one participants (14 LLD+Frail and 17 Never-depressed+Robust). MEASUREMENT: LLD was diagnosed by a geriatric psychiatrist according to the Diagnostic and Statistical Manual of Mental Disorders 5th edition for single episode or recurrent major depressive disorder without psychotic features. Frailty was assessed using the FRAIL scale (0-5), classifying subjects as robust (0), prefrail (1-2), and frail (3-5). Participants underwent T1-weighted magnetic resonance imaging in which covariance analysis of subcortical volumes and vertex-wise analysis of cortical thickness values were performed to access changes in grey matter. Participants also underwent diffusion tensor imaging in which tract-based spatial statistics was used with voxel-wise statistical analysis on fractional anisotropy and mean diffusion values to assess changes in white matter (WM). RESULTS: We found a significant difference in mean diffusion values (48,225 voxels; peak voxel: pFWER=0.005, MINI coord. (X,Y,Z) = -26,-11,27) between the LLD-Frail group and comparison group. The corresponding effect size (f=0.808) was large. CONCLUSION: We showed the LLD+Frailty group is associated with significant microstructural changes within WM tracts compared to Never-depressed+Robust individuals. Our findings indicate the possibility of a heightened neuroinflammatory burden as a potential mechanism underlying the co-occurrence of both conditions and the possibility of a depression-frailty phenotype in older adults.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Tipo de estudo: Guideline / Observational_studies / Risk_factors_studies Limite: Aged / Humans Idioma: En Ano de publicação: 2023 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Tipo de estudo: Guideline / Observational_studies / Risk_factors_studies Limite: Aged / Humans Idioma: En Ano de publicação: 2023 Tipo de documento: Article